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Ron Hochstenbach

Showing results (41-50 of 51) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2009
A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorderBert van der Zwaag, Wouter G Staal, Ron Hochstenbach, et al.
Stem Cell Research|April 23, 2009
TGF-beta1 induces efficient differentiation of human cardiomyocyte progenitor cells into functional cardiomyocytes in vitroMarie-José Goumans, Teun P de Boer, Anke M Smits, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 30, 2023
DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorderKathleen Rooney, Liselot van der Laan, Slavica Trajkova, et al.
Cell Reports|December 16, 2014
Genomic and functional overlap between somatic and germline chromosomal rearrangementsSebastiaan van Heesch, Marieke Simonis, Markus J van Roosmalen, et al.
Plos One|June 4, 2009
Gene-network analysis identifies susceptibility genes related to glycobiology in autismBert van der Zwaag, Lude Franke, Martin Poot, et al.
American Journal of Medical Genetics. Part A|May 25, 2019
Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic featuresElliot S Stolerman, Elizabeth Francisco, Jennifer L Stallworth, et al.
The Journal of Clinical Investigation|July 19, 2016
Destabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung diseaseSaskia N van der Crabben, Marije P Hennus, Grant A McGregor, et al.
HGG Advances|April 4, 2024
DNA methylation episignature and comparative epigenomic profiling for Pitt-Hopkins syndrome caused by TCF4 variantsLiselot van der Laan, Peter Lauffer, Kathleen Rooney, et al.
HGG Advances|November 6, 2024
CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignatureLiselot van der Laan, Ananília Silva, Lotte Kleinendorst, et al.
The New England Journal of Medicine|September 12, 2008
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypesHeather C Mefford, Andrew J Sharp, Carl Baker, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2009
A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorderBert van der Zwaag, Wouter G Staal, Ron Hochstenbach, et al.
Stem Cell Research|April 23, 2009
TGF-beta1 induces efficient differentiation of human cardiomyocyte progenitor cells into functional cardiomyocytes in vitroMarie-José Goumans, Teun P de Boer, Anke M Smits, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 30, 2023
DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorderKathleen Rooney, Liselot van der Laan, Slavica Trajkova, et al.
Cell Reports|December 16, 2014
Genomic and functional overlap between somatic and germline chromosomal rearrangementsSebastiaan van Heesch, Marieke Simonis, Markus J van Roosmalen, et al.
Plos One|June 4, 2009
Gene-network analysis identifies susceptibility genes related to glycobiology in autismBert van der Zwaag, Lude Franke, Martin Poot, et al.
American Journal of Medical Genetics. Part A|May 25, 2019
Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic featuresElliot S Stolerman, Elizabeth Francisco, Jennifer L Stallworth, et al.
The Journal of Clinical Investigation|July 19, 2016
Destabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung diseaseSaskia N van der Crabben, Marije P Hennus, Grant A McGregor, et al.
HGG Advances|April 4, 2024
DNA methylation episignature and comparative epigenomic profiling for Pitt-Hopkins syndrome caused by TCF4 variantsLiselot van der Laan, Peter Lauffer, Kathleen Rooney, et al.
HGG Advances|November 6, 2024
CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignatureLiselot van der Laan, Ananília Silva, Lotte Kleinendorst, et al.
The New England Journal of Medicine|September 12, 2008
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypesHeather C Mefford, Andrew J Sharp, Carl Baker, et al.
Pageof 6